DCR- Writing a Clinical Research Protocol

Sponsored by the MGH Division of Clinical Research

This course is intended for investigators and research staff. A well written protocol is essential to successful and compliant clinical research. This course will address the following questions:
• What are the required elements of a protocol including GCP requirements?
• What makes a protocol effective?
• What issues related to protocol writing have been identified in regulatory inspection and audits?
• Are there special considerations when writing a protocol?
• What is required for protocol training?

Speaker: Pamela Richtmyer, Director, Mass General Brigham Human Research Quality Improvement Program